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USP Sex Enhance Amino Tadalafil 385769-84-6 For Breast Cancer

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USP Sex Enhance Amino Tadalafil 385769-84-6 For Breast Cancer
 
Amino Tadalafil Basic Info.:
 
Product Name: Amino Tadalafil
Synonyms: Amino Tadanafil
CAS: 385769-84-6
MF: C21H18N4O4
MW: 0
EINECS: N/A
Melting point: 280-282°C
storage temp.: -20°C Freezer
Chemical Properties: White Solid
Usage: A drug analog of Tadalafil
Product Categories: Drug Analogues;Intermediates & Fine Chemicals;Pharmaceuticals
 
Amino Tadalafil Description:
 
A high-pressure liquid chromatography-diode array detection and multi-mode ionization tandem mass spectrometry (HPLC-DAD-MMI-MS/MS) method was used to identify amino-tadalafil and rimonabant in electronic cigarette (e-cigarette) cartridges. Amino-tadalafil is a drug analogue of the commercially approved ™ (i.e. tadalafil). Rimonabant is a drug that was, at one time, approved for weight loss in Europe (although approval has been retracted), but not in the United States. In addition, poor quality control over the e-cigarette products analyzed here is shown by the presence of nicotine in products labeled as containing no nicotine or by the presence of significant amounts of rimonabant oxidative degradant in e-cigarette products containing rimonabant. Identification was accomplished by comparing the retention time of relevant peaks in the sample with those of standard compounds, in addition to comparison of the UV spectra, mass spectra and/or product ion mass spectra.
 
Function Of Amino Tadalafil:
 
Made of natural soybean oil residue extraction. Is the cell membrane of the active material, especially exists in the brain cells.
The main function is to improve the function of nerve cells, adjust the transmission of nerve impulses, enhance memory function, due to its strong lipotropy, absorbed quickly through the blood brain barrier into the brain, help relax vascular smooth muscle cells, increase the role of brain blood flow.
 

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1-(4-(Benzyloxy)-6-METHOXYBENZOFURAN-2-yl)-2-bromoethanone. 98%

Product Name: 1-(4-(Benzyloxy)-6-methoxybenzofuran-2-yl)-2-bromoethanone.
CAS Number: 1476847-52-5
Purity:≥98%
Formula: C8H10N2O2
Molecular weight: 166.18
DeliveryTime: 3-5 days after received your deposit
Port: Tianjin
Production Capacity: 50 Kilogram/Week
Storage: Keep away from fire and heat source

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96-48-0 GBL Intermediate GBL Wheel Cleaner Gamma Butyrolactone

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96-48-0 GBL Intermediate GBL Wheel Cleaner Gamma Butyrolactone
 
Gamma Butyrolactone Basic Info.:
 
Product Name: Gamma-Butyrolactone
Alias: Gamma Butyrolactone, 1, 4- Butyrolactone, γ -Butyroladone, GBL, BLO
CAS: 96-48-0
MF: C4H6O2
MW: 86.09
Einecs: 202-509-5
Purity : 99.5%
Melting Point:-44°C
Boiling Point:206°C
Flash Point:99.2°C
Ignition temperature:455°C
Refractive Index:nd20 :1.434~1.440
Density 1.12 g/mL at 25 °C(lit. )
Storage temp. 2-8°C
Chemical Properties: Colorless clear oily liquid with acetone-like odor
 
Gamma Butyrolactone Description:
 
Gamma-Butyrolactone (γ-butyrolactone or GBL) is a hygroscopic colorless liquid with a weak characteristic odor which is soluble in water. GBL is a common solvent and reagent in chemistry as well as being used as a flavouring, as a cleaning solvent, as a superglue remover, and as a solvent in some wet aluminium electrolytic capacitors. In humans it acts as a prodrug for GHB, and it is used as a recreational intoxicant with effects similar to alcohol.
 
GBL has been found in extracts from samples of unadulterated wines. This finding indicates that GBL is a naturally occurring component in some wines and may be present in similar products. The concentration detected was approximately 5 μg/mL and was easily observed using a simple extraction technique followed by GC/MS analysis. GBL can be found in cheese flavourings but typically results in a content of 0.0002% GBL in the final foodstuff.
 
GBL is a lactone. It is hydrolyzed under basic conditions, for example in a sodium hydroxide solution into sodium gamma-hydroxybutyrate, the sodium salt of gamma-hydroxybutyric acid. Under acidic conditions it forms an equilibrium mixture of both compounds. These compounds then may go on to form a polymer. When treated with a non-nucleophilic base, like lithium diisopropylamide, GBL can become an alpha-carbon nucleophile. The related compound caprolactone can be used to make a polyester in this manner.
GBL is not active in its own right; its mechanism of action stems from its identity as a prodrug of GHB. The hypnotic effect of GHB is enhanced by combination with alcohol. A 2003 rat study showed that GBL in combination with ethanol showed a potentiated hypnotic effect, as the sleep-timing measure was longer than both of the individual components combined.
 
GBL is rapidly converted into GHB by paraoxonase (lactonase) enzymes, found in the blood. Animals which lack these enzymes exhibit no effect from GBL. GBL is more lipophilic (fat soluble) than GHB, and so is absorbed faster and has higher bioavailability. Because of these pharmacokinetic differences, GBL tends to be more potent and faster-acting than GHB, but has a shorter duration; whereas the related compound 1,4-butanediol (1,4-B) tends to be slightly less potent, slower to take effect but longer-acting than GHB.
 
Gamma Butyrolactone Uses:
 
(1) GBL can be used to produce a-pyrrolidone, 1-Methyl-2-pyrrolidinone , polyvinyl pyrrolidone, and α-Acetyl-γ-butyrolactone, etc.
(2) GBL can be used as anaesthetic and tranquilizer, used to produce ciprofloxacin and interferon, as the intermediate of vitamin and rolicyprine;
(3) GBL is the intermediate of plant growth stimulator and insecticide.
(4) GBL is a good antioxidant, plasticizer, extractant, adsorbent, dispersant, fixative and curing agent; Moreover, it can also be used in battery, capacitor and development of color film.
 

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Anabolic Steroid Raw Powder Androsta-1, 4-Diene-3, 17-Dione USP

Androsta-1,4-diene-3,17-dione (Steroids)  
 
Basic Info.
Model NO.:897-06-3                                                Type:Chemical Reagent
Molecular Formula:C19H24O2                                  Molecular Weight:284.39 
Assay: 99%                                                            Export Markets:Global
Function:Hormones and Regulation of Endocrine Function of Drug, Anesthetic and Adjuvant, Blood System Agents, Cardiovascular Agents, Urinary System Agents, Respiratory System Agents
 
Additional Info.
Packing:5kg/tin                                                     Origin:China
EINECS: 212-977-2                          Standard:USP28
Appearance: Nearly white crystalline powder, soluble in alcohol, insoluble
HS Code:2937290018
Usage: Simplified hormonal drugs, from the testis or urine extracted with the role of a male hormone steroids, norethisterone, testis
 
OUR ADWANTAGE: 
1, High quality with competitive price: 
1)Standard: Enterprise Standard
2)We are manufacturer and can provide high quality products with factory price.
 
2, Fast and safe delivery
1)Parcel can be sent out in 24 hours after payment. Tracking number available
2)Secure and discreet shipment. Various transportation methods for your choice.
3)Customs pass rate ≥99%
4) We have our own agent/remailer/distributor who can help us ship our products very fast and safe, and we have stock in there for transferring.
 
3, We have clients throughout the world. 
1)Professional service and rich experience make customers feel at ease, adequate stock and fast delivery meet their desire.
2)Market feedback and goods feedback will be appreciated, meeting customers's requirement is our responsibility.
3) High quality, competitive price, fast delivery, first-class service gain the trust and praise from the customers
 
If you need this or you are interest in this kind of products, you are free to send me email or call me directly, we can talk more about the details of the products.
No matter you become a customer to me or not at last, you are welcome to inquire from me!
 
Tel: +86-731-22290218
Fax: +86-731-22290218
Cell: +8618188938027
E-mail: YCWlb031@yccreate.com
Skype:andyjake@outlook.com(Andy Xu)
 
 

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High Quality Anti-Estrogen Steroids Raloxifene HCl 82640-04-8

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High Quality Anti-Estrogen Steroids Raloxifene HCl 82640-04-8 
 
Raloxifene HCL Basic Info.:
 
Product Name: Raloxifene Hydrochloride
Synonyms: Raloxifene HCL;Raloxifene Hydrochloride;Ly156758;Piperidin;Keoxifene;Keoxifene Hydrochloride;Ly 139481;AKOS 92138
CAS: 82640-04-8
MF: C28H28ClNO4S
MW: 510.04
Melting Point: 250-253°C
Storage Temp.: -20°C Freezer
Solubility DMSO: 28 mg/mL, soluble
Chemical Properties: Light-Yellow Solid
Assay: 99%
Grade: Pharmaceutical Grade
Product Categories: Active Pharmaceutical Ingredients;Raloxifene;Intracellular receptor;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;Pharmaceutical intermediate;API;Inhibitors;antifungal
Usage: amino acid, nutrient, Labeled Raloxifene, intended for use as an internal standard for the quantification of Raloxifene by GC- or LC-mass spectrometry.A nonsteroidal, selective estrogen receptor modulator (SERM). Antiosteoporotic.
 
Product Description:
 
Raloxifene HCL(marketed as Evista) is an oral selective estrogen receptor modulator (SERM) that has estrogenic actions on bone and anti-estrogenic actions on the uterus and breast. It is used in the prevention of osteoporosis in postmenopausal women and to reduce the risk of invasive breast cancer in postmenopausal women with osteoporosis and in postmenopausal women at high risk for invasive breast cancer.
 
This drug is different from hormones (including estrogens and progestins). It works by acting like estrogen (as a selective estrogen receptor modulator or SERM) in some parts of the body. Raloxifene HCL helps to preserve bone mass, but it does not affect the breast and uterus like estrogen or relieve symptoms of menopause such as hot flashes.
 
Raloxifene HCL is indicated for the treatment and prevention of osteoporosis in postmenopausal women. It is also used for reduction of risk and treatment of invasive breast cancer, and it also reduces breast density.For either osteoporosis treatment or prevention, supplemental calcium and/or vitamin D should be added to the diet if daily intake is inadequate.
 
Raloxifene HCL is used to prevent and treat bone loss (osteoporosis) in women after menopause. Maintaining strong bones by slowing bone loss helps to reduce the risk of fractures.
 
Raloxifene HCL may also lower the chance of getting a certain type of breast cancer (invasive) in women after menopause.
 

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Injectable Steroid Oil Liquid Mass 500 Mg/Ml For Body Building

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Injectable Steroid Oil Liquid Mass 500 Mg/Ml For Body Building
 
Mass 500 Basic Info.:
 
Product Name: Mass 500
1ml Mass 500 contains:
200mg Testosterone Decanoate,
150mg Boldenone Undecylenate,
150mg Nandrolone Decanoate
 
Product Description Of Mass 500:
 
Testosterone Decanoate:
Testosterone decanoate is a steroid hormone from the androgen and is found in mammalsand other vertebrates, testosterone decanoate is primarily secreted in the tests of mailsand the ovaries of female, although small amount are also secreted by the adrenal glands,testosterone decanoate is the principle male sex hormone and an anabolic steroid.Testosterone decanoate plays a key role in the development of male reproductive tissue,such as the testis and prostates. In addition, testosterone decanoate is essential for health and well-being as well as the prevention of osteoporosis, testosterone decanoateis conserved through most vertebrates, although fish make a slightly difference from called 11-ketotestosterone.
 
Boldenone Undecylenate: 
Boldenone Undeclynate is an anabolic steroid developed for veterinary use, mostly for treatment of horses. In the US it is not indicated for use in humans and is only available through veterinary clinic. The activity of boldenone is mainly anabolic, with a low androgenic potency.
Boldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys.
 
Nandrolone Decanoate: 
Nandrolone decanoate is a popular steroid which is structurally similar to testosterone, minus a carbon atom at the 19th position. This creates a steroid that exhibits less androgenic properties compared to that of Testosterone, resulting in the conversion to a weaker metabolite- dihydronandrolone, not DHT. Androgenic related side effects are still possible, but are likely to be of a less occurrence compared to that of the likes of testosterone. The compound is usually referred to as 'deca' as deca-durabolin was the brand name by Organon for their nandrolone decanoate.
 
Mass 500 Application:
 
We only use USP/BP standard steroid powders, oil and solvents to make steroid injections. only offer semi-finished steroid injections. You just need to buy some syringe filters To filter it before injection. Heating semi-finished steroid injections to 20ºC will make Filtering smoother.
 

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Lidocaine HCL 73-78-9 Natural Procaine Lidocaine Hydrochloride

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Lidocaine HCL 73-78-9 Natural Procaine Lidocaine Hydrochloride
 
Lidocaine HCL Basic Info.:
 
Product name: Lidocaine HCl
Alias: Lidocaine Hydrochloride
CAS No.: 73-78-9
Molecular Formula: C14H23ClN2O
Molecular Weight: 270.8
EINECS: 200-803-8
Appearance: White crystalline powder
Melting point: 80-82°C
Usage: To enhance the growing of man genitals.
 
Product Description Of Lidocaine HCL:
 
Lidocaine, as a local anesthetic, is characterized by a rapid onset of action and intermediate duration of efficacy. Therefore, lidocaine is suitable for infiltration, block and surface anesthesia. Longer-acting substances such as bupivacaine are sometimes given preference for subdural and epidural anesthesias. Lidocaine, on the other hand, has the advantage of a rapid onset of action. It can stop Epinephrine  vasoconstricts arteries form bleeding, and it can also delays the resorption of lidocaine, almost doubling the duration of anaesthesia. For surface anesthesia several formulations are available that can be used e. G. For endoscopies, before intubations etc. Buffering the pH of lidocaine makes local freezing less painful. Lidocaine drops can be used on the eyes for short ophthalmic procedures.
 
Lidocaine HCL Applications:
 
Topical lidocaine has been shown in some patients to relieve the pain of postherpetic neuralgia (a complication of shingles), though there is not enough study evidence to recommend it as a first-line treatment. IV lidocaine also has uses as a temporary fix for tinnitus. Although not completely curing the disorder, it has been shown to reduce the effects by around two thirds.
Lidocaine hydrochloride injection administered intravenously or intramuscularly, is specifically indicated in the acute management of ventricular arrhythmias such as those occurring in relation to acute myocardial infarction, or during cardiac manipulation, such as cardiac surgery.
 

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Male Enhancement 4-Androstenedione 63-05-8 For Muscle Building

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Male Enhancement 4-Androstenedione 63-05-8 For Muscle Building
 
Androstenedione Basic Info.
 
Product Name: Androstenedione
Synonyms: 4-Androstenedione;4AD;3,17-Dioxoandrost-4-Ene;delta-(sup4)-Androsten-3,17-dione;delta(Sup4)-Androstene-3,17-dione;delta4-androsten-3,17-dione;delta-4-androstenedione;SKF 2170;skf2170;4-AD
CAS: 63-05-8
MF: C19H26O2
MW: 286.41
EINECS: 200-554-5
Purity: 98.88%
Manufacturer: Kafen
Characters: Near white crystalline powder, soluble in ethanol, insoluble in water
 
Androstenedione Applications:
 
Testo-ster-one precursor and metabolite with androgenic activity. Controlled substance (anabolic steroid); Simplified hormone drugs, from the testis or urine extracted with the role of a male hormone steroids, norethisterone, testosterone propionate in the middle body, is widely used in small rheumatoid arthritis, diuretic, and a variety of contraceptive to control infectious inflammation.
 
Androstenedione Description:
 
4-Androstenedione can be synthesized in one of two ways. The primary pathway involves conversion of 17-hydroxypregnenolone to dehydroepiandrosterone by way of 17,20-lyase, with subsequent conversion of dehydroepiandrosterone to 4-Androstenedione via the enzyme 3-β-hydroxysteroid dehydrogenase. The secondary pathway involves conversion of 17-hydroxyprogesterone, most often a precursor to cortisol, to 4-androstenedione directly by way of 17,20-lyase. Thus, 17,20-lyase is required for the synthesis of 4-androstenedione, whether immediately or one step removed.  
 
The production of adrenal 4-Androstenedione is governed by ACTH, whereas production of gonadal 4-Androstenedione is under control by gonadotropins. In premenopausal women, the adrenal glands and ovaries each produce about half of the total 4-androstenedione(about 3 mg/day). After menopause, 4-androstenedione production is about halved, due primarily to the reduction of the steroid secreted by the ovary. Nevertheless, 4-androstenedione is the principal steroid produced by the postmenopausal.
 

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Manufacturer Terlipressin Acetate With High Quality 14636-12-5

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Manufacturer Terlipressin Acetate With High Quality 14636-12-5
 
Terlipressin Acetate Basic Info.:
 
Product Name: Terlipressin Acetate
Synonyms: Terlipressin;Terlipressin Acetate;Terilipressin;
CAS: 14636-12-5
MF: C52H74N16O15S2
MW: 1227.37
EINECS: 238-680-8
Product Categories: Amino Acid Derivatives;Peptide;hormones
Usage: Terlipressin is an analogue of vasopressin used as a vasoactive drug in the management of hypotension. Terlipressin is used norepinephrine-resistant septic shock and hepatorenal syndrome. Terlipressin is also used in the treatment of acute variceal bleeding.
 
Terlipressin Acetate Pharmacological Effects:
 
Terlipressin is a novel long-acting synthetic vasopressin reagent,its chemical name is three glycyl lysine vasopressin, it is a prodrug, itself has no activity ,in vivo  , it removes three glycyl residues in its N-terminus by aminopeptidase, and slowly "releases" the active lysine vasopressin. It is this "slow release" mechanism that makes it maintain the smooth muscle contraction up to 10 hours after a single administration, whereas the same dose of vasopressin, it can maintain its activity for 20-40 minutes. On the other hand,because of the slow digestion,  lysine vasopressin in the circulation cannot reach toxic levels, and usage of  terlipressin is safer.
Pharmacological effect of terlipressin is splanchnic vascular smooth muscle contraction, and reduction of visceral blood flow (such as reducing blood flow in the mesentery, spleen, uterus, etc.), thereby reducing portal vein blood flow,and reducing portal pressure, on the other hand it may also reduce plasma renin concentration, thereby increasing the renal blood flow in patients with hepatorenal syndrome, to improve kidney function, and increase urine output. Terlipressin is currently the only drug which is able to increase mortality in patients with esophageal varices bleeding , it is previously mainly used in clinical for the treatment of variceal bleeding, in addition,terlipressin now has also been successfully used for liver and kidney integrated syndrome and refractory shock, it is also likely to play a useful role in the cardiopulmonary resuscitation . Compared with vasopressin, it has a lasting effect, and it does not cause dangerous complications, including promoting  fibrinolysis and severe complications in the cardiovascular systems, and the use of it is simple (available intravenous injection), it is more suitable for rescue and treatment of emergent and critical  patients.
 
Terlipressin Acetate Mechanism of Action:
 
Terlipressin, a synthetic triglycyl-lysine derivative of vasopressin, is a inactive prodrug. It has pressor and antidiuretic effects. Following IV injection, lysine vasopressin are released following the enzymatic cleavage of 3 glycyl moieties.
Duration: 4-6 hr.
 

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N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-imino-2-phenazinamine 95%

Name   N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-imino-2-phenazinamine
Synonyms   B 628; B 628 (pharmaceutical)
copyRight
Molecular Structure   CAS # 102262-55-5, N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-imino-2-phenazinamine, B 628, B 628 (pharmaceutical)
 
Molecular Formula   C24H16Cl2N4
Molecular Weight   431.32
CAS Registry Number   102262-55-5

 

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